P.126 An unlikely impersonator of primary brain tumours: Illustrative case report and literature review of primary angiitis of the central nervous system

MW Elder, K. Chornenka, S. Marzoughi, MF Hassanabad, M. Rizzuto
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Abstract

Background: Primary angiitis of the central nervous system (PACNS) is a rare inflammatory condition affecting the parenchymal and leptomeningeal vessels of the CNS. PACNS presenting as a solitary mass lesion (ML-PACNS) constitutes a rare subtype of this pathology. Herein we present the first case reported in Canada of ML-PACNS, presenting with clinical and radiographic findings consistent with a high grade glial neoplasm, as well as a review of the literature on ML-PACNS. Methods: Review of the literature from 1987-2023 was conducted using PubMed to identify features of ML-PACNS and possible treatment paradigms. Results: A number of case reports of ML-PACNS were identified, as well as 6 retrospective analyses of a total of 67 patients. Features such as faster rate of symptom onset, and investigations such as MRI vessel-wall imaging and MR spectroscopy were suggested for identification of ML-PACNS. Treatment was highly variable, but followed guidelines for other neuroinflammatory disorders. Conclusions: Preoperative differentiation between ML-PACNS and CNS neoplasms is difficult due to their similar clinical and radiographic features. However, making this distinction is crucial as PACNS mass lesions can regress entirely with immunosuppressive therapy, potentially obviating the requirement for surgical intervention. Beyond diagnostics, further research is required to establish and validate a treatment paradigm.
P.126 原发性脑肿瘤的假冒者:中枢神经系统原发性血管炎的说明性病例报告和文献综述
背景:中枢神经系统原发性血管炎(PACNS)是一种影响中枢神经系统实质血管和脑膜血管的罕见炎症。以单发肿块病变(ML-PACNS)形式出现的原发性中枢神经系统血管炎是该病症的一种罕见亚型。在此,我们介绍了加拿大报告的首例 ML-PACNS 病例,该病例的临床和影像学表现与高级别胶质肿瘤一致,我们还回顾了有关 ML-PACNS 的文献。研究方法使用PubMed对1987-2023年的文献进行回顾,以确定ML-PACNS的特征和可能的治疗模式。结果:研究发现了多篇关于 ML-PACNS 的病例报告,以及对 67 名患者进行的 6 项回顾性分析。研究人员提出了一些识别 ML-PACNS 的特征,如症状出现的速度较快,以及核磁共振血管壁成像和核磁共振波谱成像等检查方法。治疗方法千差万别,但都遵循其他神经炎症性疾病的治疗指南。结论由于 ML-PACNS 和中枢神经系统肿瘤具有相似的临床和影像学特征,因此术前很难将两者区分开来。然而,由于 PACNS 肿块病变在接受免疫抑制治疗后可完全消退,从而有可能避免手术干预的要求,因此这种区分至关重要。除了诊断,还需要进一步的研究来建立和验证治疗模式。
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